Jiao Wenlian, Wen Ju, Li Na, Ou Ting, Qiu Changyu, Ji Yutong, Lin Kai, Liu Xiaojiao, Xie Jie
State Key Laboratory of Resource Insects, College of Sericulture, Textile and Biomass Science, Southwest University, No.2 Tiansheng Road, Beibei District, Chongqing, 400715, China.
Guangxi Key Laboratory of Sericultural Genetic Improvement and Efficient Breeding, Guangxi Zhuang Autonomous Region Sericultural Technology Promotion Station, Nanning, Guangxi Zhuang Autonomous Region, 530007, China.
Arch Microbiol. 2024 Apr 15;206(5):213. doi: 10.1007/s00203-024-03935-3.
Mulberry bacterial wilt disease, caused by Ralstonia pseudosolanacearum, is a devastating soil-borne disease in the silk-mulberry-related industry. In this study, through high-throughput sequencing, we compared the rhizosphere bacterial composition of the mulberry-resistant cultivar (K10) and susceptible cultivar (G12), confirming Bacillus as a genus-level biomarker for K10. Next, twelve Bacillus spp. isolates, derived from the rhizosphere of K10, were screened for their antagonistic activity against R. pseudosolanacearum. The isolate showing strong antagonism was identified as B. velezensis K0T24 and selected for further analysis. The fermentation supernatant of B. velezensis K0T24 significantly inhibited the growth of R. pseudosolanacearum (82.47%) and the expression of its pathogenic genes. Using B. velezensis K0T24 in mulberry seedlings also increased defense enzyme activities and achieved a control efficacy of up to 55.17% against mulberry bacterial wilt disease. Collectively, our findings demonstrate the potential of B. velezensis K0T24 in suppressing mulberry bacterial wilt disease.
由青枯雷尔氏菌引起的桑细菌性枯萎病是桑蚕相关产业中一种毁灭性的土传病害。在本研究中,通过高通量测序,我们比较了桑树抗病品种(K10)和感病品种(G12)的根际细菌组成,确定芽孢杆菌属是K10的属级生物标志物。接下来,从K10根际分离出12株芽孢杆菌属菌株,筛选它们对青枯雷尔氏菌的拮抗活性。表现出强拮抗作用的菌株被鉴定为贝莱斯芽孢杆菌K0T24,并选择进行进一步分析。贝莱斯芽孢杆菌K0T24的发酵上清液显著抑制了青枯雷尔氏菌的生长(82.47%)及其致病基因的表达。在桑树苗中使用贝莱斯芽孢杆菌K0T24还提高了防御酶活性,并对桑细菌性枯萎病实现了高达55.17%的防治效果。总的来说,我们的研究结果证明了贝莱斯芽孢杆菌K0T24在抑制桑细菌性枯萎病方面的潜力。